Use of 13C as an Indirect Tag in 15N Specifically Labeled Nucleosides. Syntheses of [8-13C-1,7,NH2-15N3]Adenosine, -Guanosine, and Their Deoxy Analogues-Reference-Cited by-同舟云学术

Use of 13C as an Indirect Tag in 15N Specifically Labeled Nucleosides. Syntheses of [8-13C-1,7,NH2-15N3]Adenosine, -Guanosine, and Their Deoxy Analogues

Published:2003-10-01 Issue:22 Volume:68 Page:8657-8661
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shallop Anthony J.¹,Gaffney Barbara L.¹,Jones Roger A.¹

Affiliation:

1. Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0345446

Reference36 articles.

1. Novel method for NMR spectral correlation between the native and the denatured states of a protein. Application to ribonuclease A

2. Nitrogen-15-labeled oligodeoxynucleotides. 3. Protonation of the adenine N1 in the A.cntdot.C and A.cntdot.G mispairs of the duplexes {d[CG(15N1)AGAATTCCCG]}2 and {d[CGGGAATTC(15N1)ACG]}2

3. Nitrogen-15-labeled 5S RNA. Identification of uridine base pairs in Escherichia coli 5S RNA by proton-nitrogen-15 multiple quantum NMR

4. Nitrogen-15-labeled oligodeoxynucleotides. 7. Use of nitrogen-15 NMR to probe hydrogen bonding in an O6MeG.cntdot.C base pair

5. Nitrogen-15-labeled oligodeoxynucleotides. 8. Use of 15N NMR to probe Hoogsteen hydrogen bonding at guanine and adenine N7 atoms of a DNA triplex

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